EP1589064A1 - Verwendung eines doppelseitig klebend ausgerüsteten Schaumstoff-Klebebands zum Befestigen von strukturierten Flachleitungen insbesondere auf Untergründen wie die Innenraum-Dekorteile eines Pkws, insbesondere Dachhimmel, Türseitenteil, Kofferraumdeckel - Google Patents
Verwendung eines doppelseitig klebend ausgerüsteten Schaumstoff-Klebebands zum Befestigen von strukturierten Flachleitungen insbesondere auf Untergründen wie die Innenraum-Dekorteile eines Pkws, insbesondere Dachhimmel, Türseitenteil, Kofferraumdeckel Download PDFInfo
- Publication number
- EP1589064A1 EP1589064A1 EP05102688A EP05102688A EP1589064A1 EP 1589064 A1 EP1589064 A1 EP 1589064A1 EP 05102688 A EP05102688 A EP 05102688A EP 05102688 A EP05102688 A EP 05102688A EP 1589064 A1 EP1589064 A1 EP 1589064A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- double
- fixing
- structured
- lid
- boot
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R16/00—Electric or fluid circuits specially adapted for vehicles and not otherwise provided for; Arrangement of elements of electric or fluid circuits specially adapted for vehicles and not otherwise provided for
- B60R16/02—Electric or fluid circuits specially adapted for vehicles and not otherwise provided for; Arrangement of elements of electric or fluid circuits specially adapted for vehicles and not otherwise provided for electric constitutive elements
- B60R16/0207—Wire harnesses
- B60R16/0215—Protecting, fastening and routing means therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D1/00—Containers having bodies formed in one piece, e.g. by casting metallic material, by moulding plastics, by blowing vitreous material, by throwing ceramic material, by moulding pulped fibrous material, by deep-drawing operations performed on sheet material
- B65D1/02—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents
- B65D1/0223—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents characterised by shape
- B65D1/023—Neck construction
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D41/00—Caps, e.g. crown caps or crown seals, i.e. members having parts arranged for engagement with the external periphery of a neck or wall defining a pouring opening or discharge aperture; Protective cap-like covers for closure members, e.g. decorative covers of metal foil or paper
- B65D41/02—Caps or cap-like covers without lines of weakness, tearing strips, tags, or like opening or removal devices
- B65D41/04—Threaded or like caps or cap-like covers secured by rotation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
- C09J7/26—Porous or cellular plastics
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
- C09J2423/006—Presence of polyolefin in the substrate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2433/00—Presence of (meth)acrylic polymer
Definitions
- the invention relates to the use of a double-sided adhesive Foam adhesive tapes for fastening structured flat cables in particular on substrates such as the interior decorative parts of a car, in particular headliner, Door side part, trunk lid in the car interior.
- the object of the invention is to provide an adhesive tape that is safe Fixation of structured and / or profiled flat cables, in particular on substrates like the interior decorative parts of a car, in particular roof lining, door side part, Boot lid allowed, which is easy to apply and that from the
- the prior art has known disadvantages.
- the invention relates to the use of a double-sided adhesive Adhesive tape with a carrier layer of PE foam, wherein the PE foam a compression hardness of less than 300 kPa at a compression of 50% (measured after ISO 844) for the attachment of structured and / or profiled flat cables preferably in the interior of passenger cars.
- a compressive strength is a force necessary to move a foam around to compress a certain height (50% of the normal height). It becomes relevant influenced by the molecular structure of the cell walls.
- a cover is present, which preferably consists of an LDPE film.
- Liners made of LDPE are known to be particularly cuddly and flexible, so that these find extensive use.
- the adhesives consist of resin-blended acrylate compositions which should have a high shear strength. These are mentioned, for example, in D. Satas [Handbook of Pressure Sensitive Adhesive Technology, 1989, published by VAN NOSTRAND REINHOLD, New York].
- alkyl group which may preferably be used for the radical R 2 , mention may hereinafter be made of butyl, pentyl, hexyl, heptyl, octyl, isooctyl, 2-methylheptyl, 2-ethylhexyl -, nonyl, decyl, dodecyl, lauryl, or stearyl (meth) acrylate or (meth) acrylic acid.
- the stamping process is excellent when using a pressure-sensitive adhesive which is up to 35 wt .-% based on comonomers in the form of vinyl compounds, in particular one or more vinyl compounds selected from the following group: Vinyl esters, vinyl halides, vinylidene halides, nitriles of ethylenically unsaturated hydrocarbons.
- vinyl compounds selected from the following group: Vinyl esters, vinyl halides, vinylidene halides, nitriles of ethylenically unsaturated hydrocarbons.
- acrylic compounds with functional groups also fall under the name "vinyl compound”.
- Such functional group-containing vinyl compounds are maleic anhydride, styrene, styrene compounds, vinyl acetate, (meth) acrylamides, N-substituted (meth) acrylamides, ⁇ -acryloyloxypropionic acid, vinylacetic acid, fumaric acid, crotonic acid, aconitic acid, dimethylacrylic acid, trichloroacrylic acid, itaconic acid, vinyl acetate, hydroxyalkyl (meth) acrylate, (meth) acrylates containing amino groups, hydroxy-containing (meth) acrylates, particularly preferably 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and / or 4-hydroxybutyl (meth) acrylate and functionalized with double bond photoinitiators; the list above is exemplary only and not exhaustive.
- the composition of the corresponding monomers is selected such that the resulting adhesives according to D. Satas [Handbook of Pressure Sensitive Adhesive Technology, 1989, VAN NOSTRAND REINHOLD, New York] have pressure-sensitive adhesive properties.
- the glass transition temperature of the acrylic PSA should, for example below 25 ° C.
- the extrusion coating is preferably carried out by an extrusion die.
- the extrusion dies used can come from one of the following three categories: T-die, fishtail die and stirrup nozzle.
- the individual types differ in the shape of their flow channel.
- For the production of oriented acrylic PSAs it is particularly preferred to coat a carrier with a stirrup nozzle in such a way that a polymer layer is formed on the carrier by a relative movement from nozzle to carrier.
- the time between the coating and the crosslinking is favorably very low, preferably not greater than 10 s.
- the free radical polymerization can be carried out in the presence of an organic solvent or in the presence of water or in mixtures of organic solvents and water or in bulk. Preferably, as little solvent as possible is used.
- the polymerization time is - depending on the conversion and temperature - between six and 48 h.
- Solvents used in the solvent polymerization are preferably esters of saturated carboxylic acids (such as ethyl acetate), aliphatic hydrocarbons (such as n-hexane or n-heptane), ketones (such as acetone or methyl ethyl ketone), petroleum ether, or mixtures of these solvents.
- carboxylic acids such as ethyl acetate
- aliphatic hydrocarbons such as n-hexane or n-heptane
- ketones such as acetone or methyl ethyl ketone
- petroleum ether or mixtures of these solvents.
- the emulsifiers and stabilizers known to the person skilled in the art are added for the polymerization.
- polymerization initiators customary radical-forming compounds such as peroxides, azo compounds and peroxosulphates are used. Initiator mixtures can also be used.
- the molecular weight of the acrylate PSAs is advantageously between 650,000 and 2,000,000 g / mol, more preferably between 700,000 and 1,000,000 g / mol.
- the polymerization is carried out in polymerization, which are generally provided with a stirrer, several feed vessels, reflux condenser, heating and cooling and are equipped for working under N 2 atmosphere and pressure.
- the polymerization medium under reduced Pressure removed, this process at elevated temperatures, for example in the range of 80 to 150 ° C is performed.
- the polymers can then in a solvent-free state, in particular as a hotmelt PSA.
- the polymers of the invention in substance manufacture.
- the polymers can be modified in the usual way.
- tackifying resins such as terpene, terpene phenol, C 5 , C 9 , C 5 / C 9 hydrocarbon, pinene, indene or rosin resins can also be added in combination.
- plasticizers various fillers (for example fibers, carbon black, zinc oxide, titanium dioxide, micro-solid beads, solid or hollow glass beads, silica, silicates, chalk, blocking-free isocyanates), anti-aging agents, light stabilizers, antiozonants, fatty acids, plasticizers, nucleating agents, blowing agents and / or or accelerators are used as additives.
- crosslinkers and promoters can be mixed for crosslinking.
- Suitable crosslinkers for electron beam crosslinking are, for example, difunctional or polyfunctional acrylates, difunctional or polyfunctional isocyanates or difunctional or polyfunctional epoxides.
- the pure or blended acrylate hotmelts are passed through a variable nozzle Slot width coated on the substrate and then with the carrier Hardened electron beams.
- the networking takes place immediately after inline operation applying the PSA to the carrier.
- Particular preference is given to using as a carrier layer of PE foams which have a Compressive hardness at a compression of 50% (measured to ISO 844) less than 150 kPa exhibit.
- the PE foams used can be characterized as follows: Volume weight [kg / m 3 ] 50 to 90 preferably 67 Tensile strength, longitudinal [kPa] - ISO 1926 800 to 1000 preferably 895 Elongation at break, longitudinal [%] - ISO 1926 150 to 200 preferably 180 Compression hardness [kPa] - ISO 844 Compression 10% 25 to 45 preferably 36 Compression 25% 50 to 70 preferably 60 Compression 50% 120 to 160 preferably 140
- the product design according to the invention also allows the processor under the aforementioned more difficult working conditions for the gluing one more safe spontaneous attachment of the new structured flat cables without special Care and very high pressure on the car headliner.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Details Of Indoor Wiring (AREA)
Abstract
Description
Diese haben wegen der Profilierung eine sehr schwierig zu verklebende Oberfläche.
Es werden von der Klebmasse für die leichte Montage oft eine hohe Anfassklebkraft und hohe Sofortklebkräfte gefordert. Andererseits ist für die Dauerbelastung im Fahrzeugleben eine sehr scherfeste Klebmasse zur sicheren Befestigung der Flachleitung notwendig. Aus klebtechnischer Sicht sind dies widersprüchliche Anforderungen, die immer nur durch einen Kompromiss realisiert werden können.
Dadurch kommt dem Wirkprinzip des Andruckes immer eine besondere Bedeutung zu.
Bei der Befestigung von Flachleitungen zum Beispiel in PKW-Dachhimmeln wird zunächst das doppelseitige Klebeband auf den Dachhimmel mit dem Applikator aufgebracht. Hierbei besteht die Aufgabe, dem Leitungsverlauf möglicht präzise folgen zu können. Die bei Flachleitungen notwendigen rechtwinkligen Verzweigungen lassen sich normalerweise nur durch Absetzen und erneutes Ansetzen nachkleben. Diese bedeutet entsprechend lange Zykluszeiten pro Verklebung, die auch bei einer Teil-Automatisierung besonders kritisch sind.
Diese Zykluszeiten lassen sich deutlich verkürzen, wenn das doppelseitige Klebeband in sehr engen Radien verklebt werden kann, und der Applikator so nicht bei jeder Abzweigung ab- und wieder angesetzt werden muss.
Diese werden zum Beispiel im D. Satas [Handbook of Pressure Sensitive Adhesive Technology, 1989, Verlag VAN NOSTRAND REINHOLD, New York] erwähnt.
- welche durch eine radikalische Polymerisation erhältlich ist,
- welche zu mindestens 65 Gew.-% auf zumindest einem acrylischen Monomer aus der Gruppe der Verbindungen der folgenden allgemeinen Formel basiert:
bei welcher das mittlere Molekulargewicht der Haftklebemasse mindestens 650.000 beträgt,
und welche, sofern sie auf einen Träger aufgetragen ist, eine Vorzugsrichtung besitzt, wobei der in Vorzugsrichtung gemessene Brechungsindex nMD größer ist als der in einer Richtung senkrecht zur Vorzugsrichtung gemessene Brechungsindex nCD, und wobei die Differenz Δn = nMD - nCD mindestens 1×10-5 beträgt.
Vinylester, Vinylhalogenide, Vinylidenhalogenide, Nitrile ethylenisch ungesättigter Kohlenwasserstoffe.
Im Sinne der Verwendung fallen auch Acrylverbindungen mit funktionellen Gruppen unter die Bezeichnung "Vinylverbindung". Solche funktionelle Gruppen enthaltenden Vinylverbindungen sind Maleinsäureanhydrid, Styrol, Styrol-Verbindungen, Vinylacetat, (Meth)acrylamide, N-substituierte (Meth)acrylamide, β-Acryloyloxypropionsäure, Vinylessigsäure, Fumarsäure, Crotonsäure, Aconitsäure, Dimethylacrylsäure, Trichloracrylsäure, Itaconsäure, Vinylacetat, Hydroxyalkyl(meth)acrylat, aminogruppenhaltige (Meth)acrylate, hydroxygruppenhaltige (Meth)acrylate, besonders bevorzugt 2-Hydroxyethyl(meth)acrylat, 2-Hydroxypropyl-(meth)acrylat, und/oder 4-Hydroxybutyl(meth)acrylat und mit Doppelbindung funktionalisierte Photoinitiatoren; die vorstehende Aufzählung ist nur beispielhaft und nicht abschließend.
- Polymerisation eines Gemisches enthaltend zumindest ein Monomer auf Vinyl-, Acryl- oder Methacrylbasis oder eine Kombination dieser Monomere, wobei das mittlere Molekulargewicht der entstehenden Polymere oberhalb von 650.000 liegt,
- anschließender Extrusionsbeschichtung der Polymermasse ,
- anschließender Vernetzung der Polymermasse auf dem Träger durch Bestrahlung mit Elektronenstrahlen.
Die Zeitdauer zwischen der Beschichtung und der Vernetzung ist in günstiger Weise sehr gering, bevorzugt nicht größer als 10 s.
Durch die Ausformung des Acrylathotmelts in der Bügel-Düse sowie den Austritt aus der Düse mit einer bestimmten Filmdicke, durch die Reckung des Haftklebemassenfilms beim Übertrag auf das Trägermaterial auf eine dünnere Filmdicke und durch die anschließende Inline-Vernetzung wird die Orientierung erhalten.
Die freie radikalische Polymerisation kann in Gegenwart eines organischen Lösungsmittels oder in Gegenwart von Wasser oder in Gemischen aus organischen Lösungsmitteln und Wasser oder in Substanz durchgeführt werden. Bevorzugt wird so wenig Lösungsmittel wie möglich eingesetzt. Die Polymerisationszeit beträgt - je nach Umsatz und Temperatur - zwischen sechs und 48 h.
Bei der Lösungsmittelpolymerisation werden als Lösemittel vorzugsweise Ester gesättigter Carbonsäuren (wie Ethylacetat), aliphatische Kohlenwasserstoffe (wie n-Hexan oder n-Heptan), Ketone (wie Aceton oder Methylethylketon), Siedegrenzbenzin oder Gemische dieser Lösungsmittel verwendet. Für die Polymerisation in wässrigen Medien bzw. Gemischen aus organischen und wässrigen Lösungsmitteln werden zur Polymerisation die dem Fachmann zu diesem Zwecke bekannten Emulgatoren und Stabilisatoren zugesetzt. Als Polymerisationsinitiatoren werden übliche radikalbildende Verbindungen wie beispielsweise Peroxide, Azoverbindungen und Peroxosulfate eingesetzt. Auch Initiatorgemische können verwendet werden. Bei der Polymerisation können weitere Regler zur Molekulargewichtssenkung und Verringerung der Polydispersität eingesetzt werden. Als so genannte Polymerisationsregler können beispielsweise Alkohole und Ether verwendet werden. Das Molekulargewicht der Acrylathaftklebemassen liegt vorteilhaft zwischen 650.000 und 2.000.000 g/mol, mehr bevorzugt zwischen 700.000 und 1.000.000 g/mol.
Raumgewicht [kg/m3] | 50 bis 90 | bevorzugt 67 |
Zugfestigkeit, längs [kPa] - ISO 1926 | 800 bis 1000 | bevorzugt 895 |
Reißdehnung, längs [%] - ISO 1926 | 150 bis 200 | bevorzugt 180 |
Stauchhärte [kPa] - ISO 844 | ||
Stauchung 10% | 25 bis 45 | bevorzugt 36 |
Stauchung 25% | 50 bis 70 | bevorzugt 60 |
Stauchung 50% | 120 bis 160 | bevorzugt 140 |
Dies ist insbesondere vorteilhaft, weil sich besagte Acrylatklebemassen aufgrund ihrer Eigenschaften seit vielen Jahren gerade in der Automobilindustrie für die Langzeitbefestigung von Teilen im PKW-Innenraum bewährt haben.
Claims (4)
- Verwendung eines doppelseitig klebend ausgerüsteten Klebebandes mit einer Trägerschicht aus PE-Schaum, wobei der PE-Schaum eine Stauchhärte von kleiner 300 kPa bei einer Stauchung von 50 % (gemessen nach ISO 844) aufweist, zur Befestigung von strukturierten und/oder profilierten Flachleitungen vorzugsweise im Innenraum von PKW.
- Verwendung nach Anspruch 1, dadurch gekennzeichnet, dass auf einer Seite des Klebebands eine Abdeckung vorhanden ist, die vorzugsweise aus einer LDPE-Folie besteht.
- Verwendung nach Anspruch 1 oder 2, dadurch gekennzeichnet, dass die Klebmasse eine harzabgemischte Acrylat-Klebemasse mit hoher Scherfestigkeit ist.
- Verwendung nach zumindest einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass die Stauchhärte bei einer Stauchung von 50 % (gemessen nach ISO 844) kleiner 150 kPa ist.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004019908A DE102004019908A1 (de) | 2004-04-21 | 2004-04-21 | Verwendung eines doppelseitig klebend ausgerüsteten Schaumstoff-Klebebands zum Befestigen von struktuierten Flachleitungen insbesondere auf Untergründen wie die Innenraum-Dekorteile eines Pkws, insbesondere Dachhimmel, Türseitenteil, Kofferraumdeckel |
DE102004019908 | 2004-04-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1589064A1 true EP1589064A1 (de) | 2005-10-26 |
EP1589064B1 EP1589064B1 (de) | 2007-02-28 |
Family
ID=34939151
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05102688A Not-in-force EP1589064B1 (de) | 2004-04-21 | 2005-04-06 | Verwendung eines doppelseitig klebend ausgerüsteten Schaumstoff-Klebebands zum Befestigen von strukturierten Flachleitungen insbesondere auf Untergründen wie die Innenraum-Dekorteile eines Pkws, insbesondere Dachhimmel, Türseitenteil, Kofferraumdeckel |
Country Status (8)
Country | Link |
---|---|
US (1) | US7396061B2 (de) |
EP (1) | EP1589064B1 (de) |
JP (1) | JP4693471B2 (de) |
KR (1) | KR20060047286A (de) |
CN (1) | CN100468900C (de) |
AT (1) | ATE355326T1 (de) |
DE (2) | DE102004019908A1 (de) |
ES (1) | ES2281879T3 (de) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2914312A1 (fr) * | 2007-03-29 | 2008-10-03 | Didier Couvreur | Ruban adhesif de masquage de pieces |
WO2010033586A2 (en) * | 2008-09-16 | 2010-03-25 | Ecolab Inc. | Use of hydroxycarboxylates for water hardness control |
CN101633824B (zh) * | 2009-08-21 | 2011-06-15 | 烟台新牟电缆有限公司 | 一种用于通信电缆物理发泡的粘结剂 |
US9477059B2 (en) | 2012-02-08 | 2016-10-25 | 3M Innovative Properties Company | Application of a continuous substrate with segmented adhesive |
US8852729B1 (en) | 2013-03-15 | 2014-10-07 | Davinci Engineering & Consulting, Llc | Seep resistant masking material |
DE102016002587A1 (de) * | 2016-03-04 | 2017-09-07 | Seton Autoleather Gmbh | Sitzbezug aus Leder für einen Fahrzeugsitz |
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DE19910730A1 (de) * | 1998-03-12 | 1999-10-14 | Certoplast Vorwerk & Sohn Gmbh | Klebeband |
DE19940229A1 (de) * | 1999-08-25 | 2001-03-08 | Valeo Beleuchtung Deutschland | Kabelsatz, insbesondere zur Verwendung in Fahrzeugen |
WO2001056777A1 (en) * | 2000-02-02 | 2001-08-09 | Sylvester Michael S | Doubled-sided self-adhesive reinforced foam tape |
WO2005039006A1 (de) * | 2003-10-17 | 2005-04-28 | Tesa Ag | VERFAHREN ZUM VERKLEBEN VON KABELBÄUMEN AUF UNTERGRÜNDEN WIE DIE INNENRAUM-DEKORTEILE EINES PKWs, INSBESONDERE DACHHIMMEL, TÜRSEITENTEIL, KOFFERRAUMDECKEL |
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DE9016999U1 (de) * | 1990-12-17 | 1992-04-16 | Beiersdorf Ag, 2000 Hamburg, De | |
US5516581A (en) * | 1990-12-20 | 1996-05-14 | Minnesota Mining And Manufacturing Company | Removable adhesive tape |
FR2706724B1 (fr) * | 1993-06-15 | 1997-04-30 | Saint Gobain Vitrage Int | Liaison électrique d'un vitrage. |
JPH0748548A (ja) * | 1993-08-03 | 1995-02-21 | Sekisui Chem Co Ltd | 感圧性接着テープ |
JPH07138542A (ja) * | 1993-11-17 | 1995-05-30 | Sekisui Chem Co Ltd | 建築内装材固定用両面粘着テープ |
JPH07331188A (ja) * | 1994-06-07 | 1995-12-19 | Sekisui Chem Co Ltd | 両面粘着テープの使用方法 |
SE503770C2 (sv) * | 1995-02-06 | 1996-08-26 | Hans Alveskog | Förfarande och anordning för att applicera dubbelhäftande tejp på föremål, samt användning därav |
JP3660740B2 (ja) * | 1996-02-27 | 2005-06-15 | 積水化学工業株式会社 | 加圧接着型両面粘着シート及び粘着剤積層装飾ボード |
JP4047434B2 (ja) * | 1998-02-13 | 2008-02-13 | 日東電工株式会社 | 粘着シ―ト類 |
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JP2002112441A (ja) * | 2000-10-02 | 2002-04-12 | Furukawa Electric Co Ltd:The | フラットケーブル用クリップおよび該クリップを用いた配索構造 |
DE10138350A1 (de) * | 2001-08-04 | 2003-02-20 | Tesa Ag | Verwendung eines doppelseitig klebend ausgerüsteten Klebebands zum Verschließen und Öffnen von Kartons oder kartonähnlichen Verpackungen |
JP2003147292A (ja) * | 2001-11-13 | 2003-05-21 | Sekisui Chem Co Ltd | 両面粘着テープ |
EP1361162B1 (de) * | 2002-05-08 | 2005-08-24 | tesa AG | Verwendung eines doppelseitig klebend ausgerüsteten Klebebands zum Verschliessen und Öffnen von Kartons oder kartonähnlichen Verpackungen |
US20050000632A1 (en) * | 2003-05-23 | 2005-01-06 | Tesa Ag | Method of bonding flat ribbon cables adhesively to substrates such as the interior decorative components of a passenger car, especially roof lining, door side part and boot lid |
-
2004
- 2004-04-21 DE DE102004019908A patent/DE102004019908A1/de not_active Withdrawn
-
2005
- 2005-04-06 AT AT05102688T patent/ATE355326T1/de not_active IP Right Cessation
- 2005-04-06 ES ES05102688T patent/ES2281879T3/es active Active
- 2005-04-06 EP EP05102688A patent/EP1589064B1/de not_active Not-in-force
- 2005-04-06 DE DE502005000408T patent/DE502005000408D1/de active Active
- 2005-04-07 CN CNB2005100638193A patent/CN100468900C/zh not_active Expired - Fee Related
- 2005-04-08 JP JP2005112441A patent/JP4693471B2/ja not_active Expired - Fee Related
- 2005-04-18 US US11/108,565 patent/US7396061B2/en not_active Expired - Fee Related
- 2005-04-20 KR KR1020050032828A patent/KR20060047286A/ko not_active Application Discontinuation
Patent Citations (4)
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DE19910730A1 (de) * | 1998-03-12 | 1999-10-14 | Certoplast Vorwerk & Sohn Gmbh | Klebeband |
DE19940229A1 (de) * | 1999-08-25 | 2001-03-08 | Valeo Beleuchtung Deutschland | Kabelsatz, insbesondere zur Verwendung in Fahrzeugen |
WO2001056777A1 (en) * | 2000-02-02 | 2001-08-09 | Sylvester Michael S | Doubled-sided self-adhesive reinforced foam tape |
WO2005039006A1 (de) * | 2003-10-17 | 2005-04-28 | Tesa Ag | VERFAHREN ZUM VERKLEBEN VON KABELBÄUMEN AUF UNTERGRÜNDEN WIE DIE INNENRAUM-DEKORTEILE EINES PKWs, INSBESONDERE DACHHIMMEL, TÜRSEITENTEIL, KOFFERRAUMDECKEL |
Non-Patent Citations (1)
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Also Published As
Publication number | Publication date |
---|---|
CN1691448A (zh) | 2005-11-02 |
JP4693471B2 (ja) | 2011-06-01 |
EP1589064B1 (de) | 2007-02-28 |
DE502005000408D1 (de) | 2007-04-12 |
ATE355326T1 (de) | 2006-03-15 |
DE102004019908A1 (de) | 2005-11-17 |
US7396061B2 (en) | 2008-07-08 |
JP2005307208A (ja) | 2005-11-04 |
KR20060047286A (ko) | 2006-05-18 |
CN100468900C (zh) | 2009-03-11 |
ES2281879T3 (es) | 2007-10-01 |
US20050236871A1 (en) | 2005-10-27 |
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